Home NDC 57687-225 Bach Original Flower Remedies Rock Rose
Product NDC 57687-225
11-digit product format 576870225
Labeler code 57687
Product ID 57687-225_ea240330-bb55-4970-e053-2a95a90aef97
Type HUMAN OTC DRUG
Nonproprietary name Helianthemum nummularium
Dosage form SOLUTION
Route ORAL
Labeler Nelson Bach USA Limited
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2022-09-20
Substance HELIANTHEMUM NUMMULARIUM FLOWER
Active strength 5 [hp_X]/.095mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Bach Original Flower Remedies Rock Rose
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HELIANTHEMUM NUMMULARIUM FLOWER 5 [hp_X]/.095mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 51BRR32WPP Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 57687-225-10 Bach Original Flower Remedies Rock Rose 10 mL in 1 BOTTLE, DROPPER SOLUTION 10 1 57687-225-10 Bach Original Flower Remedies Rock Rose 1 in 1 CARTON SOLUTION 1 1 57687-225-10 Bach Fear No More Bravery Kit 1 in 1 CARTON SOLUTION 5 [hp_X] in 0.095mL 1 57687-225-10 Bach Fear No More Bravery Kit 10 mL in 1 BOTTLE, DROPPER SOLUTION 10 mL 5 [hp_X] in 0.095mL 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 57687-225 BACH FEAR NO MORE BRAVERY KIT (ASPEN, CHERRY PLUM, ROCK ROSE) KIT [NELSON BACH USA LIMITED] 1 Current NDC, Legacy NDC 20231101_066bc3ce-69ce-fba8-e063-6394a90ac463.zip 57687-225 BACH ORIGINAL FLOWER REMEDIES ROCK ROSE (HELIANTHEMUM NUMMULARIUM) SOLUTION [NELSON BACH USA LIMITED] 1 Current NDC, Legacy NDC, 2 package rows 20221004_ea240330-bb54-4970-e053-2a95a90aef97.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 57687-225-10 57687022510 1 BOTTLE, DROPPER in 1 CARTON (57687-225-10) / 10 mL in 1 BOTTLE, DROPPER 2022-09-20 0000-00-00 No No Current